Expired Study
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Salt Lake City, Utah 84109


Purpose:

This randomized controlled trial will evaluate whether the use of pharmacogenetic testing through a Medication Therapy Management (MTM) program has a beneficial impact on drug therapy problems. More specifically, cytochrome DNA testing, which provides information with regards to participant specific metabolism of medications, will be used in the evaluation of participant medication regimens. The overall aim of the project is to evaluate if the addition of genetic CYP testing to a standardized MTM Program provides increased clinical value. To answer this question, the investigators will look at the drug therapy problems (DTPs) identified by the genetic test compared to those DTPs discovered without the test.


Study summary:

All study participants will receive a Comprehensive Medication Review (CMR). One third will have standard MTM conducted. Another third of the participants will be randomized to MTM plus drug interaction risk analysis via YouScript software. The remaining third will be randomized to MTM along with drug interaction risk analysis via YouScript software and genetic testing. The software will identify polypharmacy patients who may benefit from pharmacogenetic testing based on their current medication regimen. Results of the testing will be mailed to both the participant and their provider. Participants who undergo testing will also receive a follow-up phone call. All participants, including those who receive MTM alone, will receive a contact 3 months later to assess quality of life.


Criteria:

Inclusion Criteria: - Aged 65 or over and enrolled in a Medicare Part-D Prescription Drug Plan. - Currently prescribed ≥6 chronic medications. - Have ≥3 chronic disease states including osteoarthritis, rheumatoid arthritis, heart failure, diabetes, dyslipidemia, hypertension, asthma, chronic obstructive pulmonary disease, atrial fibrillation, and coronary artery disease. - Participant incurred the Medicare-mandated dollar amount in medication-related costs in the previous quarter. Exclusion Criteria: - Inability to perform MTM encounter due to living situation (e.g. patient is enrolled in hospice, or is in long term care facility). - Patient is unable to perform MTM encounter due to metal health barriers as described by Brief Interview for Mental Status (BIMS) score of <13 points. - Patient identifies themselves as being unable to perform the oral swab function of the genetic test. - Patient had a known MTM session within the preceding 12 months.


NCT ID:

NCT02428660


Primary Contact:

Principal Investigator
Jonathan W Magness, PharmD
VRx Pharmacy Services


Backup Contact:

N/A


Location Contact:

Salt Lake City, Utah 84109
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: November 18, 2019

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